That’s lazy
The Health and Social Care Committee’s evaluation of palliative care in England was published yesterday.
It’s hugely important, not least in the context of the assisted dying bill.
It’s had almost no media coverage.
committees.parliament.uk/publications...
Examples of solutions have existed for several years (eg @iownhs.bsky.social ambulance service, @nhswalesexecutive.bsky.social Wales ambulance service) so why are these not being taken up by other areas?
New open access article in Supportive Care in Cancer: Medicinal cannabis for symptom control in advanced cancer: a double-blind, placebo-controlled, randomised clinical trial of 1:1 tetrahydrocannabinol and cannabidiol
link.springer.com/article/10.1...
#SuppOnc #PallOnc
Improving palliative and end-of-life care has never been more important.
I am thrilled to announce the Impact Centre for Palliative and End-of-Life Care, which will accelerate better care for dying people by closing the gap between evidence and practice.
www.kcl.ac.uk/news/half-of...
Also 🦚
Dulce et decorum est pro patria mori
That pathway already exists - medical school
5p
Jamilla is absolutely right!
Being poor, old damp housing, social isolation etc etc
Suffering happens in multiple domains, all of which badly need addressed
Unfortunately, I think you could be right. If AD at its heart is considered a treatment for intolerable suffering, it will be hard to restrict it to arbitrary parameters - especially the prognosis estimate
The oversimplification of the #AD debate is troubling. There are no 'goodies' & 'baddies' here, only people: with varying experience of living & dying, some with professional insights into applying law to medicine in complex circs, or into the myriad ways people & medicine respond to illness.
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It’s been an honour to make this programme.
Thanks for everyone who spoke to us.
Timely report into current planning & coordination of end of life care: National Confidedential Enq into Pt Outcomes & Death shows gaps in services, breaching 2019 NICE guidance for commissioning & providing adequate, timely planning & delivery of #EoL care & access to palliative care teams.
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And about 46m can’t think of a bigger waste of time
Inevitable
$525 😳
It’s our responsibility as docs to empower patients to make informed decisions & plan ahead. To do that properly means taking the time to discuss options. Also, I think terms like ‘refusal’ carry a lot of negative connotations & is often an unfair way to describe often reasonable, personal decisions
Don’t you think there’s a distinction between stopping trying to keep someone alive (allowing natural death) vs actively killing someone? It’s the difference between asking someone to stop doing something to you vs asking someone to do something to you. Quite different I think
Have you read Andrew Grey’s piece on conceptions of dignity in this debate? My opposition is collective and communitarian - not religious or libertarian. www.theosthinktank.co.uk/research/202...
Article from Prof Mark Taubert on the process of assisted dying / suicide. There is a reason why in Canada, where lethal drugs can be administered both orally and intravenously (IV), that the vast majority of people opt for IV.
www.spectator.co.uk/article/the-...